Tag | Content |
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EnhancerAtlas ID | HS147-23867 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr2:167965950-167967160 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr2:167966682-167966692 | TTTAATTAGA | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr2:167966009-167966024 | TGAACTCCTGACCTC | - | 6.22 | POU2F2 | MA0507.1 | chr2:167966408-167966421 | TTAATTTGCATGT | + | 6.5 | TP53 | MA0106.3 | chr2:167966488-167966506 | GACATGTCTGTTCATGTC | + | 6.09 | TP53 | MA0106.3 | chr2:167966488-167966506 | GACATGTCTGTTCATGTC | - | 6.17 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 167966123 | 167966580 | chr2 | 167966617 | 167966760 |
| Enhancer Sequence | CAGCTAATTT TTGTATTTTT AGTAGAGACA GAGTTTCTCC ATGTTGGCCA AGCTGGTCTT 60 GAACTCCTGA CCTCAGGTGA TCTGCCCACC TTGGCCTCCC AAAGTCCTGG GATTACAGGC 120 ATGAGCCACT GTGCCCTGGC CAACCACATT TTCTTTAACC AGTCTAACGT TCATGGGCAT 180 TTATGTTGAT TCCATGTCTT TGCTGTTGTG AATAGCGCTG CGATGAACAT ATATATGCAT 240 GTGTCTTTGT GGTAGAACAA TTTCTATTCC TTTGGGTATA TACCTAATAA TGGGATTGCT 300 GGGAAAGCCA TTGCTTTCTA CAGTGGTTGA GCTAATTTAC AATCTCACCA GCAGTGTGTA 360 AGCATTCCCT TTTCTCCACT ACCTCATCAG CATCTGTTAT TTTTTTCTTT TTAGTAATAG 420 CCATTCTTAC TGGTATGAGA TGGTATCTCT TTGTGGTTTT AATTTGCATG TCTCTAATGA 480 TTAGTGATGT TGAGCTTTTT TTCATGTGCT TGTTGGCCAC ATGTATGTCT TCTTTTGAGA 540 CATGTCTGTT CATGTCCTTT GCCCACTTCT TCAGGGGTTG TTTGATTTTT ACTTGTAAAT 600 TTGTTTAAGT TCCTTGTAGA TTCTGTATAT TAGACCTTTG TTGGATGCAT AGTTTGTAAA 660 TATTTTCTCC TATTCCGTAA GTTGTCTGTT TACTCTGTTG ATAGTTTCTT TTGTTGTGCA 720 GAAATTCTTT TATTTAATTA GATCCTATTT GTTAATTTTT TTCCTTGCAA TTGCTTTGGA 780 ATCTTCATCA TGAAATCTTG CCAAATCTTA TGCCCACAAT GGTATTTCCA AGCTTATCTC 840 CCAGAGTTTT CATAGTTTTA AGTTTTACAT TAAAGTCTTT AATCCATCTG GAGTTGATTT 900 TTGTATGTAG TATAAGGTAA GGGTCCAGTT TCATTCTTCT GTGTTTGGCT AGCCAGTTAT 960 CCCAACACAA TTTATTGAAT GGGGAATCCT TTCTTCATTG CTTGTTTTTG TCAGCTTTGT 1020 CAAAGATCAG ATGGTTGTAG GTGTGCAACC TTATTTCTGT ACTCTCTATT CTGTTCCATT 1080 AGTCTATGTG TCTGTCTGTT TTTGTACCAG TAGCATGCTG CCTTGGTTAC AGTAGCCCTC 1140 TAATATAGTT TGAAGTCTGG TAATGTGATG CCTCCAGCTT TGTTCTTTTT GCTTTGGATT 1200 GTCTTGGCTA 1210
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